Grzybek Gabriela, Wasiłek Olga, Greluk Magdalena, Słowik Grzegorz, Davó-Quiñonero Arantxa, Bueno-López Agustín, Lozano-Castelló Dolores, Stelmachowski Paweł, Zasada Filip, Piskorz Witold, Kotarba Andrzej
Faculty of Chemistry, Jagiellonian University in Krakow, Gronostajowa 2, 30-387 Krakow, Poland.
Faculty of Chemistry, Maria Curie-Sklodowska University, Maria Curie-Sklodowska Sq. 3, 20-031 Lublin, Poland.
ACS Appl Mater Interfaces. 2025 Feb 5;17(5):7697-7706. doi: 10.1021/acsami.4c18402. Epub 2025 Jan 22.
Hydrogen, a sustainable and environmentally friendly fuel, can be obtained through the ethanol steam reforming (ESR) process. The most promising catalysts for this process are those based on non-noble metals such as cobalt. The activity, selectivity, and stability of these catalysts strongly depend on the presence of alkali dopants. In this work, we have taken on the challenge of understanding the role of alkali. We synthesized a series of cobalt-containing catalysts supported on α-alumina and doped with Na, K, Rb, and Cs, which were thoroughly characterized using spectroscopic and microscopic techniques. We elucidated the significant difference in the efficiency of undoped and alkali-doped catalysts, based on diffuse reflectance infrared Fourier transform (DRIFT) operando spectroscopy studies under ESR conditions. The catalytic test results indicated a strong effect of alkali promoters on the interaction between the acetaldehyde byproduct and the Co/α-AlO catalyst surface. Experimental data were confronted with the results of periodic DFT-GGA+U molecular modeling. It has been shown that electron transfer from alkali atoms to the cobalt active phase strongly influences the ethanol reforming pathway by increasing the adsorption energy of the aldehyde intermediate and facilitating the key C-C bond-breaking step.
氢气作为一种可持续且环境友好的燃料,可通过乙醇蒸汽重整(ESR)过程获得。该过程中最具前景的催化剂是基于钴等非贵金属的催化剂。这些催化剂的活性、选择性和稳定性很大程度上取决于碱掺杂剂的存在。在这项工作中,我们面临着理解碱的作用这一挑战。我们合成了一系列负载在α-氧化铝上并掺杂有Na、K、Rb和Cs的含钴催化剂,并使用光谱和显微镜技术对其进行了全面表征。基于ESR条件下的漫反射红外傅里叶变换(DRIFT)原位光谱研究,我们阐明了未掺杂和碱掺杂催化剂在效率上的显著差异。催化测试结果表明,碱促进剂对乙醛副产物与Co/α-AlO催化剂表面之间的相互作用有强烈影响。实验数据与周期性DFT-GGA+U分子模拟结果进行了对比。结果表明,碱原子向钴活性相的电子转移通过增加醛中间体的吸附能并促进关键的C-C键断裂步骤,强烈影响乙醇重整途径。